Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 6
rs4246215
FADS2 ; FEN1
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 6
rs4072037
MUC1
0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 4
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 3
rs2622621
ABCG2
0.851 0.240 4 88109768 intron variant C/A;G snv 3
rs314277
LIN28B
0.925 0.080 6 104959787 intron variant A/C;G;T snv 3
rs7754840
CDKAL1
0.807 0.200 6 20661019 intron variant G/A;C;T snv 3
rs8176746
ABO
0.882 0.160 9 133255935 missense variant G/A;T snv 4.1E-06; 0.12 3
rs10203853
MROH2A
1.000 0.080 2 233778772 intron variant A/G;T snv 2
rs11676348 0.790 0.160 2 218145423 regulatory region variant C/G;T snv 2
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 2
rs1500482
MROH2A
1.000 0.080 2 233774392 upstream gene variant C/A;T snv 2
rs1537372
CDKN2B-AS1
0.752 0.120 9 22103184 intron variant G/A;T snv 2
rs4242382 0.763 0.240 8 127505328 intergenic variant A/G;T snv 2
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv 2
rs7586006
MROH2A
1.000 0.080 2 233776881 intron variant T/A;G snv 2
rs10036748
TNIP1
0.752 0.360 5 151078585 intron variant C/A;T snv 1
rs1023890 1.000 0.080 4 117780291 intergenic variant G/A;C snv 1
rs12412391
LINC01475
0.790 0.080 10 99529178 intron variant A/G;T snv 1
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 1
rs13278062
LOC389641 ; TNFRSF10A
0.807 0.200 8 23225458 non coding transcript exon variant G/A;C;T snv 1
rs1427667
TNS1
1.000 0.080 2 218029404 intron variant C/G;T snv 1
rs1432096
LINC01500
1.000 0.080 14 58718338 intron variant G/A;T snv 1